US3887517A - Piperidine derivatives and their use as stabilizers - Google Patents

Piperidine derivatives and their use as stabilizers Download PDF

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US3887517A
US3887517A US404147A US40414773A US3887517A US 3887517 A US3887517 A US 3887517A US 404147 A US404147 A US 404147A US 40414773 A US40414773 A US 40414773A US 3887517 A US3887517 A US 3887517A
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Keisuke Murayama
Katsuaki Matsui
Tomoyuki Kurumada
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Sankyo Co Ltd
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D211/56—Nitrogen atoms
    • C07D211/58—Nitrogen atoms attached in position 4
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K5/00—Use of organic ingredients
    • C08K5/16—Nitrogen-containing compounds
    • C08K5/34—Heterocyclic compounds having nitrogen in the ring
    • C08K5/3412—Heterocyclic compounds having nitrogen in the ring having one nitrogen atom in the ring
    • C08K5/3432—Six-membered rings
    • C08K5/3435—Piperidines

Definitions

  • ABSTRACT Piperidine derivatives having the formula The compounds are useful as stabilizers against photoand thermal-deterioration of various synthetic polymers.
  • a piperidine derivative having the formula cyano, epoxy,-alkoxycarbonyl having l4 carbon atoms in the alkoxy moiety or phenoxycarbonyl; an alkenyl group having 3-4 carbon atoms; an alkynyl group having 3-4 carbon atoms; benzyl group; an aliphatic acyl group having 2-4'carbon atoms; an alkoxycarbonyl group having 2-9 carbon atoms or a phenylalkoxycarbonyl group having l-4 carbon atoms in the alkoxy moiety; n is l or 2 and, when n is 1, R represents hydrogen atom; an alkyl group'having l4 carbon atoms; a phenylalkyl group having 1-4 carbon atoms in the alkyl moiety; or an aryl group which may be optionally substituted with halogen, hydroxy, nitro, alkyl having l4 carbon atoms, alkoxy having l4 carbon
  • preferable compounds are 2 carbon atoms in the alkyl moiety, styryl group, a phenyl or naphthyl group whichmay be optionally substituted with halogen, hydroxy, nitro or alkali metal sulfo or 2- furyl group and, when n is 2, R represents hydrogen atom and the carbon atoms, each of which is linked to R are directly bonded.
  • R represents hydrogen atom or methyl group
  • R represents hydrogen atom, an alkyl group having 1-4 carbon atoms, a phenylalkyl group having l4 carbon atoms in the alkyl moiety or phenyl group
  • R represents an alkyl group having ll8 carbon atoms, an alkenyl group having 2-4 carbon atoms, a phenyalkyl group having 14 carbon atoms in the alkyl moiety, styryl group, a phenyl or naphthyl group which may be optionally substituted with halogen, hydroxy, nitro or alkali metal sulfo or 2-furyl.
  • the alkyl group may be exemplified by methyl, ethyl, propyl, butyl, as substituted alkyl groups, 2-hydroxyethyl, 2-ethoxyethyl, ethoxymethyl, Z-phenoxyethyl, 2- acetoxyethyl, 2-stearoyloxyethyl, Z-benzoyloxyethyl, Z-acryloyloxyethyl, 2-chloroethyl, 2-cyanoethyl, cyanomethyl, 2,3-epoxypropyl, ethoxycarbonylmethyl, butoxycarbonylmethyl, methoxycarbonylmethyl, 2- methoxycarbonylethyl, phenoxycarbonylmethyl; the alkenyl group by allyl or Z-butenyl; the alkynyl group by 2-propynyl or Z-butynyl; the phenylalkyl group by benzy
  • the alkyl group may be exemplified by methyl, ethyl, propyl, isopropyl, butyl or isobutyl; the phenylalkyl by benzyl or phenethyl; the aryl group by phenyl, aor ,B-naphthyl, or a phenyl which may be optionally substituted with bromine, chlorine, hydroxy, nitro, methyl, methoxy or sodium sulfo.
  • the alkyl group may be exemplified by methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, pentyl, l-ethylpentyl, hexyl, heptyl, actyl, dodecyl.
  • the alkylene group may be exemplified by ethylene, propylene, trimethylene or tetramethylene those having the formula (I) wherein R represents h'y- I drogen atom or an alkyl group having 1-4 carbon.
  • R represents hydrogen atom, an alkyl group having l-4 carbon atoms, a phenylalkyl group having l4 carbon atoms in the alkyl moiety or phenyl group and R represents an alkyl group having [-1 8 carbon atoms, an alkenyl group having 2-4 carbon atoms, a phenyalkyl group having 14 and the phenylene group by p-phenylene or mphenylene.
  • synthetic polymer as used in this invention is contemplated to include I polyolefin including lowand high-density polyethylene, polypropylene, polystyrene, polybut adiene, polyisoprene, other olefin homopolymer and ethylene-propylene copolymer, ethylene-butene copolymer, ethylene-vinyl acetate copolymer, styter.
  • rene-butadiene copolymer acrylonitrile styrenebutadiene copolymer, other copolymers of other ethylene-forming unsaturated monomer and olefin;
  • polyvinyl chloride and polyvinylidene chloride including homopolymers of vinyl chloride and vinylidene chloride, respectively, copolymers of vinyl chloride with vinylidene chloride, copolymers of each of vinyl chloride and vinylidene chloride with vinyl acetate or other ethylene-forming unsaturated monomer;
  • polyacetal for example, polyoxymethylene and polyoxyethylene
  • polyester for example, polyethylene terephthalate
  • polyamide for example, 6-nylon, 6,6-nylon and 6,10
  • the synthetic polymeric materials are widely utilized in the form of various shapes, e.g., fibres, films, sheets, other molded products, latex and foams, because of their excellent properties.
  • tetramethylpiperidine 28 4-benzylideneaminol -benzyl-2,2,6,6-tetramethylpiperidine 29. l-allyl-4-cinnamylideneamino-2,2,6,6-tetramethylpiperidine 30. 4( l-chloromethyl-benzylideneamino)-l-(2- propynyl)-2,2,6,6-tetramethylpiperidine 31. l,2-bis(2,2,6,6-tetramethyl-4- piperidylimino)ethane 32.
  • the piperidine derivatives l) of this invention can be readily obtained by condensing the 4-aminopiperidine derivatives (II) with an aldehyde or ketone as illustrated by the following reaction equation.
  • the reaction may be effected in a suitable inert organic solvent at room temperature or with heating.
  • n c ⁇ n .R
  • R R- R and n are the same as set forth above.
  • the piperidine derivatives (1) employed as a stabilizer may be easily incorporated into a symthetic polymeric material by various methods commonly used in the art.
  • the stabilizer may be added to a synthetic polymeric material at any stage in the manufacture of a molded product therefrom.
  • the stabilizer in a dry powder form may be admixed with a synthetic polymeric material or a suspension or emulsion of the stabilizer may be admixed therewith.
  • the amount of the piperidine derivative (1) which may be added to a synthetic polymeric material according to this invention is varied upon the kind, nature and purpose for use of the synthetic polymeric material to be stabilized.
  • the amount ranging in 0.01 5% by weight may be employed to the weight of synthetic polymeric material, but a practical range may be varied upon the synthetic polymeric material and there may be used 0.01 2.0% by weight, desirably 0.02 1.0% by weight for polyolefin; 0.01 1.0% by weight, desirably 0.02 0.5% by weight for polyvinyl chloride and polyvinylidene chloride; 0.01 5.0% by weight, desirably 0.02 2.0% by weight for polyurethane and polyamide.
  • the above-mentioned stabilizer may be used alone or in admixture with other known additives such as antioxidants, ultraviolet absorbents, light protection agents, fillers, pigments and the like.
  • ANTIOXIDANTS Simple, 2,6-dialkylphenols, such as, for example, 2,6- di-tert.butyl-4-methylphenol, 2-tert.butyl-4,6-
  • alkylated hydroquinones such as, for example, 2,5-di-tert.butyl-hydroquinone, 2,5-di-tert.- amyl-hydroquinone, 2,6-di-tert.butyl-hydroquinone, 2,5-di-tert.butyl-4-hydroxyanisole, 3,5-di-tert.butyl-4- hydroxyanisole and tris( 3 ,5-di-tert.butyl-4- hydroxyphenyl) phosphite, 3,5-di-tert.butyl-4-hydroxyphenyl-stearate, di-(3,5-di-tert.butyl-4-hydroxyphenyl)adipate.
  • alkylated hydroquinones such as, for example, 2,5-di-tert.butyl-hydroquinone, 2,5-di-tert.- amyl-hydroquinone, 2,6-di-tert.butyl-
  • Hydroxylated thiodiphenyl ethers such as, for example, 2,2 '-thiobis( 6-tert.buryl-4methylphenyl 2,2-thiobis-(4-octylphenol), 4,4-thiobis(6-tert.butyl- B-methylphenol), 4,4-thiobis(3,6-di-sec.amylphenol), 4,4-thiobis-(6-tert.butyl-2-methylphenol) and 4,4- bis(2,6-dimethyl-4-hydroxyphenyl)disulfide.
  • Alkylidene-bisphenols such as, for example, 2,2- methylene-bis(6-tert.butyl-4-methylphenol),2,2-
  • Hydroxybenzyl-aromatics such as, for example, 1,3,- 5-tri( 3 ,5 -di-tert.butyl-4-hydroxybenzyl)-2,4,6-trimethylbenzene, 1,4-di( 3,5-di-tert.butyl-4- hydroxybenzyl)-2,3,5,6-tetramethylbenzene and 2,4,6- tri-( 3 ,5-di-tert.butyl-4-hydroxybenzyl )phenol.
  • s-Triazine compounds such as, for example, 2,4-bisoctylmercapto-6-( 3 ,5 -di-tert.butyl-4-hydroxyanilino s-triazine, 2-octylmercapto-4,6-bis( 3,5-di-tert.-butyl-4- hydroxyanilino)-s-triazine, 2-octylmercapto- 4,6-bis(3,5-di-tert.butyl-4-hydroxyphenoxy)-s-triazine, 2,4,6-tris( 3 ,5-di-tert.butyl-4-hydroxyphenoxy )-striazine, 2,4,6-tris(3,5-di-tert.butyl-4-hydroxyphenylethyl)-s-triazine and l,3,5-tris-(3,5-di-tert.butyl-4- hydroxybenzyl)isocyanurate.
  • Esters of 3,5-di-tert.butyl-4-hydroxyphenylpropionic acid with monohydric or polyhydric alcohols such as, for example, methanol, ethanol, octadecanol, 1,6- hexanediol; 1,9-nonanediol, ethylene glycol, 1,2- propanediol, diethylene glycol, thiodiethylene glycol, neopentyl glycol, pentaerythritol, 3-thiaundecanol, 3- thia-pentadecanol, trimethylhexanediol, trimethylolethane, trimethylolpropane, tris-hydroxyethylisocyanurate and 4-hydroxymethyl-l-phospha-2,6,7- trioxyabicyclo[2,2,2]octane.
  • monohydric or polyhydric alcohols such as, for example, methanol, ethanol, octadecanol
  • Esters of 5-tert.butyl-4-hydroxy-3-methylphenylpropionic acid with monohydric or polyhydric alcohols such as, for example, methanol, ethanol, octadecanol, l,6-hexanediol, 1,9-nonanediol, ethylene glycol, 1,2- propanediol, diethylene glycol, thiodiethylene glyjcol, neopentyl glycol, pentaerythritol, 3-thiaundecanol, 3- thia-pentadecanol, trimethylhexanediol, trimethylolethane, trimethylolpropane, tris-hydroxyethylisocyanurate and 4-hydroxymethyl-1-phospha-2,6,7- trioxabicyclo[2,2,2]-octane.
  • monohydric or polyhydric alcohols such as, for example, methanol, ethanol, octade
  • Esters of 3,5-di-tert.butyl-4-hydroxyphenylacetic acid with monohydric or polyhydric alcohols such as, for example, methanol, ethanol, octadecanol, 1,6- hexanediol, 1,9-nonanediol, ethylene glycol, 1,2- propanediol, diethylene glycol, thiodiethylene glycol, neopentyl glycol, pentaerythritol, 3-thia-undecanol, 3- thia-pentadecanol, trimethylhexanediol, trimethylolethane, trimethylolpropane, tris-hydroxyethylisocyanurate and 4-hydroxymethyl-l-phospha-2,6,7- tri-oxabicyclo[2,2,2]octane.
  • monohydric or polyhydric alcohols such as, for example, methanol, ethanol, octadecano
  • Acylaminophenols such as, for example, N-(3,5-ditert.butyl-4-hydroxyphenyl)stearic acid amide and N,- N'-bis( 3 ,5-di-tert.butyl-4-hydroxyphenyl)-thio-bisacetamide.
  • Benzylphosphonates such as, for example, 3,5-ditert.butyl-4-hydroxybenzylphosphonic acid dimethyl ester, 3,5-di-tert.butyl-4-hydroxybenzylphosphonic acid diethyl ester, 3,5-di-tert.butyl-4-hydroxybenzylphosphonic acid dioctadecyl ester and 5-tert.butyl-4- hydroxy-3-methylbenzylphosphonic acid dioctadecyl ester.
  • Aminoaryl derivatives such as, for example, phenyll-naphthylamine, phenyl-Z-naphthylamine, N,N- diphenyl-p-phenylenediamine, N,N-di-2-naphthyl-pphenylenediamine, N,N'-di-sec.butyl-p- 7 phenylenediamine, 6-ethoxy-2,2,4-trimethyll ,2- dihydroquinoline, 6-dodecyl-2,2,4-trimethyll ,2- dihydroquinoline, monoand di-octyliminodibenzyl and polymeriaed 2,2,4-trimethyl-l,2-dihydroquinoline.
  • UV-absorbers and light protection agents 2-(2-Hydroxyphenyl)-benztriazoles, such as, for example, the -methyl-, 3',5'-di-tert.butyl-, 5'-tert.butyl- 5-( l,l,3,3-tetramethyl-butyl)-, 5-chloro-3',5'-ditert.-butyl-, 5-chloro-3 '-tert.butyl-5 '-methyl-, 3-sec.butyl-5-tert.butyl-, 3'-[a-methylbenzyl]-5'- methyl-, 3'-[a-methylbenzyl]-5'-methyl-5-chloro-, 4'- hydroxy-, 4-methoxy-, 4'-octoxy-, 3',5-di-tert.amyl-, 3'-methyl-5'-carbomethoxyethylor 5-chloro-3',5'-ditert.a
  • 2,4-Bis(2'-hydroxyphenyl)-6-alkyl-s-triazines such as, for example, the 6-ethyl-, 6-undecylor 6 heptadecylderivatives.
  • Z-Hydroxy-benzophenones such as, for example, the 4-hydroxy-, 4-methoxy-, 4-octoxy-, 4-decyloxy-, 4- dodecyloxy-, 4-benzyloxy-, 4,2-4-trihydroxyor 2'- hydr0xy-4,4-dimethoxy-derivatives.
  • 1,3-Bis(2-hydroxy-benzoyl)benzenes such as, for example
  • Esters of optionally substituted benzoic acids such as, for example, phenyl salicylate, octylphenyl, salicylate, di-benzoylresorcinol, bis(4-tert.butylbenzoyl) resorcinol, benzoyl-resorcinol, 3,5-di-tert.butyl-4- hydroxybenzoic acid 2,4-di-tert.buty1phenyl ester, octadecyl ester or 2-methyl-4,6-di-tert.butylphenyl ester.
  • benzoic acids such as, for example, phenyl salicylate, octylphenyl, salicylate, di-benzoylresorcinol, bis(4-tert.butylbenzoyl) resorcinol, benzoyl-resorcinol, 3,5-di-tert.butyl-4- hydroxybenzoic acid 2,4
  • Acrylates such as for example, a-cyano-B,,8- diphenylacrylic acid ethyl ester or isooctyl ester, a-carbomethoxycinnamic acid methyl ester, oz-cynao- B-methyl-p-methoxycinnamic acid methyl ester or butyl ester and N-(B-carbomethoxy-vinyl)-2- methylindoline.
  • Nickel compounds such as, for example, nickel complexes of 2,2-thiobis(4-tert.octylphenol), such as the 1:1 and 1:2 complex, optionally with other ligands such as n-butylamine, triethanolamine or N-cyclohexyldiethanolamine, nickel complexes of bis(4-tert.octy1- phenyl)sulphone, such as the 2:1 complex, optionally with other ligands such as 2-ethyl-caproic acid, nickel dibutyldithiocarbamate, nickel salts of 4-hydroxy-3,5- di-tert.butylbenzylphosphonic acid monoalkyl esters, such as the methyl, ethyl or butyl ester, the nickel complex of 2-hydroxy-4-methyl-phenyl-undecylketonoxime and nickel 3 ,5-di-tert.butyl-4- hydroxybenzoate.
  • ligands such as n-butylamine, tri
  • Oxalic acid diamides such as, for example, 4,4-dioctyloxyoxanilide, 2,2 '-dioctyloxy-5,5 -di-tert.- butyloxanilide, 2,2 -di-dodecyloxy-5,5 '-di-tert.- butyloxyanilide, 2-ethoxy-5-tert.butyl-2 -ethyloxanilide, 2-ethoxy-2'-ethyl-0xanilide, N,N-bis-(3- dimethylaminopropyl)oxalamide, mixture of oand pmethoxy and oand p-ethoxy-di-substituted oxanilides and mixtures of 2-ethoxy-5-tert.butyl-2'ethyloxanilide with 2-ethoxy-2-ethyl-5,4'-di-tert.butyloxanilide.
  • Metal deactivators such as. for example, oxanilide, isophthalic acid dihydrazine, sebacic acid, bisphenylhydrazide, bis-benzylidene oxalic acid dihydrazide, N,N-diacetyl-adipic acid dihydrazide, N,N-bis-salicyloyl-oxalic acid dihydrazide, N,N-bis-salicyloyl-hydrazine and N,N'-bis(3,5-ditert.butyl-4-hydroxyphenylpropionyl)hydrazine.
  • oxanilide isophthalic acid dihydrazine, sebacic acid, bisphenylhydrazide, bis-benzylidene oxalic acid dihydrazide, N,N-diacetyl-adipic acid dihydrazide, N,N-bis-salicyloyl-oxalic acid dihydra
  • Phosphites such as, for example, triphenylphosphite, di-phenyl alkyl-phosphites, phenyl dialkylphosphites, trinonylphenylphosphite, trilaurylphosphite, trioctadecylphosphite, 3,9-di-isodecyloxy2,4,8, 10- tetraoxa-3,9-diphospha-spiro[5.5]undecane and tris(4- hydroxy-3,5-di-tert.butylphenyl)phosphite.
  • Polyamide stabilizers such as, for example, copper salts in combination with iodides and/or phosphorus compounds and salts of divalent manganes.
  • Basic co-stabilizers such as, for example, polyvinylpyrrolidone, melamine, benzoguanamine, triallyl cyanurate, dicyandiamide, urea derivatives, hydrazine derivatives, amines, polyamides, polyurethanes and alkali metal salts and alkaline earth metal salts of higher saturated or unsaturated fatty acids, e.g., Ca stearate, Mg laurate, Na ricinoleate, K palmitate and Zn stearate.
  • PVC stabilizers such as, for example, organic tin compounds, organic lead compounds and C./l salts of fatty acids.
  • Nucleating agents such as, for example, 4-tert.- butylbenzoic acid, adipic acid and diphenylacetic acid.
  • additives such as, for example, plasticizers, lubricants, e.g., glycerine monostearate, emulsifiers, antistatic agents, flameproofing agents, pigments, carbon black, asbestos, glass fibres, kaolin and talc.
  • These other additives may be usually blended into a synthetic polymers at a ratio of 0.5-3 to the weight of the piperidine derivatives (1).
  • Examples 1 through 8 describe the synthetic polymeric material compositions having incorporated therein the piperidine derivative(l) and their stabilizing effects and Referential Examples 1-3 describe the preparation of the piperidine derivative (1).
  • EXAMPLE 1 Into 100 parts of polypropylene [prepared by twice recrystallization of Noblen JHH-G", trade name of Mitsui Toatsu Chemicals Inc., from monochlorobenzene] was incorporated 0.25 part of the stabilizing compound of this invention. The resulting mixture was blended and molten. The molten was molded into a sheet with a thickness of 0.5 mm. under heating and pressure.
  • the sheet was exposed to irradiation of ultraviolet ray at C. in a Fade-Meter and the time when the sheet would become brittle was measured.
  • the sheet was exposed to irradiation of ultraviolet ray at 45C. in a Fade-Meter and the time when the 7 sheet would become brittle was measured.
  • EXAMPLE 3 I lnto 100 parts of polystyrene [prepared by twice recrystallization of Styrone, trade name of AsahiDow Limited, from a mixture of benzene with methanol] wherein A YI means a change of yellowness index, YI means a yellowness index after exposure and YI means an initial yellowness index of a test piece.
  • polycaprolactone type polyurethane [E5080, trade name, available from The Nippon Elastollan Industries Ltd.] was incorporated 0.5 part of the stabilizing compound of this invention.
  • the resulting mixture was heated and melted and then molded into a sheet having a thickness of about 0.5 mm.
  • the sheet thus formed was subjected to the exposure to ultraviolet ray in a Fade-Meter at 45C. for 15 hours and then tested for the retentions of ultimate elongation and ultimate tensile strength.
  • a synthetic polymer composition stabilized against photoand thermal-deterioration wherein there is incorporated, in a sufficient amount to prevent said deterioration, a compound having the formula CH KU CH CH I? CH wherein R represents hydrogen atom; and alkyl group having 1-4 carbon atoms which may be optionally substituted with hydroxy, alkoxy having 1-4 carbon atoms, phenoxy, aliphatic acyloxy having 2-18 carbon atoms, aromatic acyloxy having 7-11 carbon atoms, halogen, cyano, epoxy, alkoxycarbonyl having 1-4 carbon atoms in the alkoxy moiety or phenoxycarbonyl; an alkenyl group having 3-4 carbon atoms; an alkynyl group having 3-4 carbon atoms; benzyl group; an aliphatic acyl group having 2-4 carbon atoms; an alkoxycarbonyl gorup having 2-9 carbon atoms or a phenylalkoxycarbonyl group having l-4 carbon atoms in
  • R represents an alkyl group having l-4 carbon atoms, a phenylalkyl group having l-4 carbon atoms in the alkyl moiety or phenyl group and R represents an alkyl group having l-18 carbon atoms, an alkenyl group having 2-4 carbon atoms, a phenylalkyl group having l-4 carbon atoms in the alkyl moiety, styryl group, a phenyl or naphthyl group which may be optionally substituted with halogen, hydroxy, nitro or alkali metal sulfo or 2- furyl group and, when n is 2, R represents hydrogen atom and the carbon atoms, each of which is linked to R are directly bonded.
  • a syntehtic polymer composition stabilized against photoand thermal-deterioration wherein there is incorporated, in a sufficient amount to prevent said deterioration, 4-benzylideneamino-2,2,6,6-tetramethylpiperidine, 4-( l-methylbenzylideneamino)-2,2,6,6- tetramethylpiperidine or 4-benzylideneaminol,2,2,6,6-pentamethylpiperidine.

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Hydrogenated Pyridines (AREA)
  • Compositions Of Macromolecular Compounds (AREA)
US404147A 1972-10-25 1973-10-09 Piperidine derivatives and their use as stabilizers Expired - Lifetime US3887517A (en)

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CH (1) CH589111A5 (enrdf_load_stackoverflow)
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Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4028334A (en) * 1973-04-11 1977-06-07 Ciba-Geigy Corporation Piperidine derivatives
US4064102A (en) * 1976-03-18 1977-12-20 American Cyanamid Company Light and heat stabilizers for polyolefins
US4066615A (en) * 1971-06-05 1978-01-03 Sankyo Company Limited Polymer compositions containing piperidine derivatives as stabilizers
US4104248A (en) * 1975-03-21 1978-08-01 Montefibre S.P.A. Polyolefine-based polymeric compositions stabilized by organic polyamines, textile fibers obtained therefrom, and novel organic polyamines
US4140673A (en) * 1976-03-23 1979-02-20 Bayer Aktiengesellschaft Piperidine derivatives as light stabilizers
US4166813A (en) * 1977-05-18 1979-09-04 Sankyo Company Ltd. Polyalkylated 4-aminopiperidine derivatives
US4182703A (en) * 1978-01-09 1980-01-08 Eastman Kodak Company Biheterocyclic ultraviolet stabilizers and their use in organic compositions
USRE30385E (en) * 1979-07-16 1980-08-26 American Cyanamid Company Light and heat stabilizers for polyolefins
US20100092386A1 (en) * 2007-04-23 2010-04-15 David Segev System for delivering therapeutic agents into living cells and cells nuclei
CN108586320A (zh) * 2018-04-24 2018-09-28 宿迁联盛科技有限公司 一种聚合型橡胶稳定剂及其制备方法

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1467672A (en) 1974-04-11 1977-03-16 Ciba Geigy Ag Stabilised epoxy resin
JPS515351A (ja) * 1974-07-03 1976-01-17 Mitsui Petrochemical Ind Horiorefuinsoseibutsuno seizohoho
JPS524546A (en) * 1975-07-01 1977-01-13 Mitsubishi Chem Ind Ltd Polyolefin composition
IT1213028B (it) * 1986-01-30 1989-12-07 Ciba Geigy Spa Composti piperidinici atti all'impiego come stabilizzanti per polimeri sintetici.

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US4066615A (en) * 1971-06-05 1978-01-03 Sankyo Company Limited Polymer compositions containing piperidine derivatives as stabilizers
US4028334A (en) * 1973-04-11 1977-06-07 Ciba-Geigy Corporation Piperidine derivatives
US4104248A (en) * 1975-03-21 1978-08-01 Montefibre S.P.A. Polyolefine-based polymeric compositions stabilized by organic polyamines, textile fibers obtained therefrom, and novel organic polyamines
US4064102A (en) * 1976-03-18 1977-12-20 American Cyanamid Company Light and heat stabilizers for polyolefins
US4140673A (en) * 1976-03-23 1979-02-20 Bayer Aktiengesellschaft Piperidine derivatives as light stabilizers
US4166813A (en) * 1977-05-18 1979-09-04 Sankyo Company Ltd. Polyalkylated 4-aminopiperidine derivatives
US4182703A (en) * 1978-01-09 1980-01-08 Eastman Kodak Company Biheterocyclic ultraviolet stabilizers and their use in organic compositions
USRE30385E (en) * 1979-07-16 1980-08-26 American Cyanamid Company Light and heat stabilizers for polyolefins
US20100092386A1 (en) * 2007-04-23 2010-04-15 David Segev System for delivering therapeutic agents into living cells and cells nuclei
CN108586320A (zh) * 2018-04-24 2018-09-28 宿迁联盛科技有限公司 一种聚合型橡胶稳定剂及其制备方法

Also Published As

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DE2365382A1 (de) 1974-10-10
IT1004620B (it) 1976-07-20
CA1008858A (en) 1977-04-19
GB1394770A (en) 1975-05-21
FR2204630B1 (enrdf_load_stackoverflow) 1976-10-01
JPS4964634A (enrdf_load_stackoverflow) 1974-06-22
NL7314720A (enrdf_load_stackoverflow) 1974-04-29
CH589111A5 (enrdf_load_stackoverflow) 1977-06-30
DE2353539A1 (de) 1974-06-12
FR2204630A1 (enrdf_load_stackoverflow) 1974-05-24

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